4097-53-4

Basic information

• Product Name: 3,5-DINITRO-BIPHENYL-4-OL
• Synonyms: 4-HYDROXY-3,5-DINITROBIPHENYL;3,5-DINITRO-BIPHENYL-4-OL;3,5-DINITROBIPHENYL;2,6-dinitro-4-phenylphenol;2,6-dinitro-4-phenyl-phenol
• CAS NO: 4097-53-4
• Molecular Formula: C₁₂H₈N₂O₅
• Molecular Weight: 260.2
• Mol File: 4097-53-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 350.3 °C at 760 mmHg
• Flash Point: 146.9 °C
• Appearance: /
• Density: 1.471 g/cm³
• Vapor Pressure: 2.19E-05mmHg at 25°C
• Refractive Index: 1.666
• CAS DataBase Reference: 3,5-DINITRO-BIPHENYL-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DINITRO-BIPHENYL-4-OL(4097-53-4)
• EPA Substance Registry System: 3,5-DINITRO-BIPHENYL-4-OL(4097-53-4)

Safety Data

• Hazardous Substances Data: 4097-53-4(Hazardous Substances Data)

Usage

General Description

3,5-DINITRO-BIPHENYL-4-OL is a chemical compound with the molecular formula C12H8N2O5. It is derived from biphenyl and contains two nitro groups and a hydroxyl group attached to the fourth carbon of one of the benzene rings. 3,5-DINITRO-BIPHENYL-4-OL is known for its high toxicity and is classified as a hazardous substance. It is not only harmful to the environment but also poses health risks to humans, with potential effects on the liver, kidneys, and nervous system. Due to its toxic nature, 3,5-DINITRO-BIPHENYL-4-OL is strictly regulated and must be handled and stored with extreme caution to prevent any adverse effects on health and the environment.

InChI:InChI=1/C12H8N2O5/c15-12-10(13(16)17)6-9(7-11(12)14(18)19)8-4-2-1-3-5-8/h1-7,15H

Upstream product

• 92-52-4 biphenyl 
• 92-69-3 4-Phenylphenol 

Downstream Products

• 1306755-09-8 C₁₂H₇N₂OS₄ 
• 62559-49-3 4-Methoxy-3,5-dinitrobiphenyl 
• 36321-62-7 4-Phenyl-2,6-dinitrochlorbenzol 
• 109559-54-8 1-nitro-3-phenyl-phenoxazine 

Relevant articles and documents

Hydroxynitrobiphenyls produced by photochemical reaction of biphenyl in aqueous nitrate solution and their mutagenicities

From the photoreaction products of biphenyl in aqueous nitrate solution, the following eight hydroxynitrobiphenyls were isolated by silica gel column chromatography and thin layer chromatography on silica gel and polyamide plates: 4-hydroxy-3,5-dinitrobiphenyl (F1(2)or), 4,2'-dihydroxy-3,3'-dinitrobiphenyl (F4(1)-3), 4-hydroxy-3,3'-dinitrobiphenyl (F4(1)-4), a hydroxydinitrobiphenyl (F4(1)-5a), 4,4'-dihydroxy-3,3'-dinitrobiphenyl (F4(1)-5b), a dihydroxydinitrobiphenyl (F4(1)-6), 2-hydroxy-3-nitrobiphenyl (F5(1)) and 4-hydroxy-3-nitrobiphenyl (F5(2)). Among these compounds, four dinitro compounds, F1(2)or, F4(1)-4, F4(1)-5a and F4(1)-6, exhibited mutagenicity toward S. typhimurium TA98 without S-9 mix. The major products in this reaction were nitrophenylphenols, F5(1) and F5(2), and these were non-mutagenic. The major mutagens, F4(1)-5a and F4(1)-6, were produced in such small amounts that the exact structures could not be determined. The mechanism of production of these hydroxynitrobiphenyls is discussed on the basis of the results of analysis of the reaction mixture by high-performance liquid chromatography.